M. James

发表

Predicting the reactivity of proteins from their sequence alone: Kazal family of protein inhibitors of serine proteinases.

S. Anderson, I. Apostol, S. Lu, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Aspartic proteinases : retroviral and cellular enzymes

M. James, 1998 .

Crystal and molecular structure of the serine proteinase inhibitor CI-2 from barley seeds.

M. James, C. Mcphalen, C. McPhalen, 1988, Biochemistry.

Structural basis of prion inhibition by phenothiazine compounds.

A. Aguzzi, M. James, P. K. Baral, 2014, Structure.

An algorithm for determining the conformation of polypeptide segments in proteins by systematic search

J. Moult, M. James, 1986, Proteins.

The TB Structural Genomics Consortium: a decade of progress.

D. Eisenberg, M. James, J. Sacchettini, 2011, Tuberculosis.

Structural comparison of two serine proteinase-protein inhibitor complexes: eglin-c-subtilisin Carlsberg and CI-2-subtilisin Novo.

M. James, C. Mcphalen, M N James, 1988, Biochemistry.

Rat submaxillary gland serine protease, tonin. Structure solution and refinement at 1.8 A resolution.

M. James, M. Fujinaga, M Fujinaga, 1987, Journal of molecular biology.

Water molecules participate in proteinase‐inhibitor interactions: Crystal structures of Leu18, Ala18, and Gly18 variants of turkey ovomucoid inhibitor third domain complexed with Streptomyces griseus proteinase B

S. Anderson, M. James, M. Laskowski, 1995, Protein science : a publication of the Protein Society.

Deleterious effects of β‐branched residues in the S1 specificity pocket of Streptomyces griseus proteinase B (SGPB): Crystal structures of the turkey ovomucoid third domain variants Ile18I, Val18I, Thr18I, and Ser18I in complex with SGPB

S. Anderson, M. Qasim, M. James, 2008, Protein Science.

A critical assessment of comparative molecular modeling of tertiary structures of proteins *

M. James, S. Mosimann, R. Meleshko, 1995, Proteins.

Molecular docking programs successfully predict the binding of a β-lactamase inhibitory protein to TEM-1 β-lactamase

J. Cherfils, R. Abagyan, I. Kuntz, 1996, Nature Structural Biology.

The crystal structure of succinyl-CoA synthetase from Escherichia coli at 2.5-A resolution.

M. James, W. T. Wolodko, M. Fraser, 1995, The Journal of biological chemistry.

Structural and kinetic characterization of a β-lactamase-inhibitor protein

André Matagne, J. Frère, M. Page, 1994, Nature.

A potent new mode of β-lactamase inhibition revealed by the 1.7 Å X-ray crystallographic structure of the TEM-1–BLIP complex

Pedro M. Alzari, M. James, P. Alzari, 1996, Nature Structural Biology.

Crystallographic analysis of transition-state mimics bound to penicillopepsin: phosphorus-containing peptide analogues.

M. James, N. Strynadka, J. Hanson, 1993, Biochemistry.

Crystal structure of human pepsin and its complex with pepstatin

M. James, M. Fujinaga, N. Tarasova, 1995, Protein science : a publication of the Protein Society.

Crystal structures of the helix-loop-helix calcium-binding proteins.

M. James, N. Strynadka, N. J. Strynadka, 1989, Annual review of biochemistry.

Molecular structure of the acyl-enzyme intermediate in β-lactam hydrolysis at 1.7 Å resolution

C. Betzel, M. James, K. Sutoh, 1992, Nature.

Lowering the entropic barrier for binding conformationally flexible inhibitors to enzymes.

M. James, M. Fraser, P. Bartlett, 1998, Biochemistry.

Comparison of the predicted model of α-lytic protease with the X-ray structure

M. James, G. Brayer, L. Delbaere, 1979, Nature.

Structure of the calcium regulatory muscle protein troponin-C at 2.8 Å resolution

M. James, O. Herzberg, Michael N. G. James, 1985, Nature.

Common structural framework of the two Ca2+/Mg2+ binding loops of troponin C and other Ca2+ binding proteins.

M. James, O. Herzberg, 1985, Biochemistry.

Refined crystal structure of Streptomyces griseus trypsin at 1.7 A resolution.

R J Read, R. Read, M. James, 1988, Journal of molecular biology.

Structural evidence for gene duplication in the evolution of the acid proteases

T. L. Blundell, T. Blundell, J. Jenkins, 1978, Nature.

Structure and refinement of penicillopepsin at 1.8 A resolution.

M. James, A. Sielecki, A R Sielecki, 1983, Journal of molecular biology.

Molecular structure of an aspartic proteinase zymogen, porcine pepsinogen, at 1.8 Å resolution

M. James, A. Sielecki, Michael N. G. James, 1986, Nature.

ADP-binding site of Escherichia coli succinyl-CoA synthetase revealed by x-ray crystallography.

M. James, W. T. Wolodko, M. Fraser, 2000, Biochemistry.

Crystal and molecular structures of the complex of α-chymotrypsin with its inhibitor Turkey ovomucoid third domain at 1.8 Å resolution

Randy J. Read, R. Read, W. Ardelt, 1987 .

Molecular docking identifies the binding of 3-chloropyridine moieties specifically to the S1 pocket of SARS-CoV Mpro

J. Vederas, M. James, Jiang Yin, 2007, Bioorganic & Medicinal Chemistry.

Thermodynamic criterion for the conformation of P1 residues of substrates and of inhibitors in complexes with serine proteinases.

S. Anderson, S. Lu, M. Qasim, 1999, Biochemistry.

Structural aspects of activation pathways of aspartic protease zymogens and viral 3C protease precursors.

M. James, A. R. Khan, N. Khazanovich-Bernstein, 1999, Proceedings of the National Academy of Sciences of the United States of America.

The molecular structure of human progastricsin and its comparison with that of porcine pepsinogen.

M. James, N. Tarasova, M. Chernaia, 1995, Advances in experimental medicine and biology.

The crystal and molecular structures of a cathepsin K:chondroitin sulfate complex.

M. James, D. Brömme, Zhenqiang Li, 2008, Journal of molecular biology.

Crystallization of Photobacterium leiognathi non-fluorescent flavoprotein, an unusual flavoprotein with limited sequence identity to bacterial luciferase.

M. James, D. O'Kane, S. Moore, 1992, Journal of molecular biology.

Aryl methylene ketones and fluorinated methylene ketones as reversible inhibitors for severe acute respiratory syndrome (SARS) 3C-like proteinase

J. Vederas, M. James, L. Eltis, 2008, Bioorganic Chemistry.

Crystal Structures of the Main Peptidase from the SARS Coronavirus Inhibited by a Substrate-like Aza-peptide Epoxide

M. James, L. Eltis, Jie Liu, 2005, Journal of Molecular Biology.

Expression, purification, crystallization and preliminary crystallographic analysis of the phosphoglycerate kinase from Acinetobacter baumannii.

M. James, Jiang Yin, C. Garen, 2012, Acta crystallographica. Section F, Structural biology and crystallization communications.

The structures of Thermoplasma volcanium phosphoribosyl pyrophosphate synthetase bound to ribose-5-phosphate and ATP analogs.

M. James, Maia M Cherney, Leonid T Cherney, 2011, Journal of molecular biology.

The molecular biology of human renin and its gene.

M. James, J. Baxter, C. Carilli, 1989, The Yale journal of biology and medicine.

X-ray crystallographic studies of the complex between porcine pepsin and the aspartic proteinase inhibitor PI-3 from the nematode Ascaris suum.

M. James, B. Dunn, M. Chernaia, 1998, Advances in experimental medicine and biology.

Expression, purification, crystallization and preliminary X-ray analysis of two arginine-biosynthetic enzymes from Mycobacterium tuberculosis.

M. James, L. Cherney, C. Garen, 2006, Acta crystallographica. Section F, Structural biology and crystallization communications.

(E)-1-(2'-deoxy-beta-D-ribofuranosyl)-2,4-difluoro-5-(2-iodovinyl)benzene.

M. James, B. Mark, J. C. Parrish, 2001, Acta crystallographica. Section C, Crystal structure communications.

Expression, purification and preliminary crystallographic analysis of Rv3002c, the regulatory subunit of acetolactate synthase (IlvH) from Mycobacterium tuberculosis.

M. James, Jiang Yin, C. Garen, 2011, Acta crystallographica. Section F, Structural biology and crystallization communications.

Expression, purification, crystallization and preliminary X-ray analysis of Rv3117, a probable thiosulfate sulfurtransferase (CysA3) from Mycobacterium tuberculosis.

M. James, R. Sankaranarayanan, L. Cherney, 2008, Acta crystallographica. Section F, Structural biology and crystallization communications.

The molecular structure of Rv2074, a probable pyridoxine 5'-phosphate oxidase from Mycobacterium tuberculosis, at 1.6 angstroms resolution.

M. James, C. Garen, M. Cherney, 2006, Acta crystallographica. Section F, Structural biology and crystallization communications.

X-ray crystallographic structure of recombinant eosinophil-derived neurotoxin at 1.83 A resolution.

D. Newton, M. James, S. Mosimann, 1996, Journal of molecular biology.

Crystal Structure of Human β-Hexosaminidase B: Understanding the Molecular Basis of Sandhoff and Tay–Sachs Disease

M. James, B. Mark, S. Knapp, 2018 .

The structure of the arginine repressor from Mycobacterium tuberculosis bound with its DNA operator and Co-repressor, L-arginine.

M. James, L. Cherney, C. Garen, 2009, Journal of molecular biology.

An algorithm which predicts the conformation of short lengths of chain in proteins

J Moult, J. Moult, M. James, 1986 .

An Episulfide Cation (Thiiranium Ring) Trapped in the Active Site of HAV 3C Proteinase Inactivated by Peptide-based Ketone Inhibitors

J. Vederas, M. James, L. Eltis, 2006, Journal of Molecular Biology.

SQ 14,225: 1-(d-3-mercapto-2-methylpropionyl)-l-proline

M. James, M. Fujinaga, 1980 .

Preliminary X-ray crystallographic analysis of sulfide:quinone oxidoreductase from Acidithiobacillus ferrooxidans.

M. James, Jianshe Liu, M. Solomonson, 2009, Acta crystallographica. Section F, Structural biology and crystallization communications.

High throughput crystallography of TB drug targets.

D. Eisenberg, J. Berger, M. James, 2007, Infectious disorders drug targets.

Crystal structure of the holotoxin from Shigella dysenteriae at 2.5 A resolution.

M. James, M. Fraser, M. Chernaia, 1994, Nature structural biology.

Molecular enzymology underlying regulation of protein phosphatase-1 by natural toxins.

M. James, C. Holmes, J. Maynes, 2002, Current medicinal chemistry.

Shiga toxin type 2

M. James, M. Fujinaga, M. Fraser, 2004 .

Crystal structure of human pepsin and its complex with pepstatin

M. James, M. Fujinaga, N. Tarasova, 1995, Protein science : a publication of the Protein Society.

Crystallization of human β-hexosaminidase B

M. James, W. B. Church, L. Swenson, 1992 .

Crystallization of glycogen debranching enzyme.

N. Madsen, M. James, K. Hayakawa, 1984, Journal of Molecular Biology.

Crystal Data for a Bacterial Serine Protease

M. James, L. Smillie, 1969, Nature.

Crystal structure of 2,4-diselenouracil.

M. James, H. Mautner, E. Shefter, 1966, Journal of pharmaceutical sciences.

Synthesis and evaluation of keto-glutamine analogues as potent inhibitors of severe acute respiratory syndrome 3CLpro.

J. Vederas, D. Wishart, M. James, 2004, Journal of medicinal chemistry.

Synthesis of pseudoxazolones and their inhibition of the 3C cysteine proteinases from hepatitis A virus and human rhinovirus-14

J. Vederas, M. James, Yeeman K. Ramtohul, 2002 .

Pseudoxazolones, a new class of inhibitors for cysteine proteinases: inhibition of hepatitis A virus and human rhinovirus 3C proteinases

J. Vederas, M. James, Yeeman K. Ramtohul, 2001 .

Preliminary X-ray crystallographic analysis of ornithine acetyltransferase (Rv1653) from Mycobacterium tuberculosis.

M. James, R. Sankaranarayanan, C. Garen, 2009, Acta crystallographica. Section F, Structural biology and crystallization communications.

Pig heart CoA transferase exists as two oligomeric forms separated by a large kinetic barrier.

M. James, J. Rochet, C. Kay, 2000, Biochemistry.

Characterization of the phosphoserine of pepsinogen using 31P nuclear magnetic resonance: corroboration of X-ray crystallographic results.

M. James, S. P. Williams, W. A. Bridger, 1986, Biochemistry.

Viral Cysteine Peptidases and Cysteine Peptidase Inhibitors

M. James, Jiang Yin, 2008 .

The crystal structure of PR3, a neutrophil serine proteinase antigen of Wegener's granulomatosis antibodies.

M. James, M. Fujinaga, M. Chernaia, 1996, Journal of molecular biology.

Crystal Structure of the Tumor-promoter Okadaic Acid Bound to Protein Phosphatase-1*

M. James, K. Bateman, C. Holmes, 2001, The Journal of Biological Chemistry.

Karplus relation and the correlation of two anomalous carbon-13 vicinal proton coupling constants with bonding electron density distribution found by accurate x-ray analysis

L. Delbaere, M. James, R. Lemieux, 1973 .

Crystallographic Analysis of a Pepstatin Analogue Binding to the Aspartyl Proteinase Penicillopepsin at 1.8 Angstroms Resolution

John Moult, J. Moult, M. James, 1994 .

Crystal Structures of Active and Inactive Conformations of a Caliciviral RNA-dependent RNA Polymerase*

M. James, K. Ng, F. Parra, 2002, The Journal of Biological Chemistry.

Crystal structure studies and inhibition kinetics of tripeptide chloromethyl ketone inhibitors with Streptomyces griseus protease B.

L. Delbaere, M. James, G. Brayer, 1980, Journal of molecular biology.

Contribution of peptide bonds to inhibitor-protease binding: crystal structures of the turkey ovomucoid third domain backbone variants OMTKY3-Pro18I and OMTKY3-psi[COO]-Leu18I in complex with Streptomyces griseus proteinase B (SGPB) and the structure of the free inhibitor, OMTKY-3-psi[CH2NH2+]-Asp19

S. Anderson, M. Qasim, M. James, 2001, Journal of molecular biology.

Why does pepsin have a negative charge at very low pH? An analysis of conserved charged residues in aspartic proteinases.

M. James, N. Andreeva, 1991, Advances in experimental medicine and biology.

Molecular and crystal structures of monoclinic porcine pepsin refined at 1.8 A resolution.

A. Fedorov, M. James, A. Boodhoo, 1990, Journal of molecular biology.

Structure of recombinant human renin, a target for cardiovascular-active drugs, at 2.5 A resolution.

J D Baxter, M. James, M. Murphy, 1989, Science.

Proteolytic Enzymes of the Viruses of the Family Picornaviridae

M. James, E. Bergmann, 1999, Proteases of Infectious Agents.

Picornaviral 3C cysteine proteinases have a fold similar to chymotrypsin-like serine proteinases

Marc Allaire, M. James, M. Allaire, 1994, Nature.

2-Phenyl-2-(1-hydroxycycloalkyl)ethylamine derivatives: synthesis and antidepressant activity.

M. James, G. Stack, G. E. Husbands, 1990, Journal of medicinal chemistry.

Synthesis and evaluation of keto-glutamine analogues as inhibitors of hepatitis A virus 3C proteinase.

J. Vederas, M. James, Yeeman K. Ramtohul, 2002, The Journal of organic chemistry.

Synthesis and Evaluation of Keto-Glutamine Analogues as Inhibitors of Hepatitis A Virus 3 C Proteinase

J. Vederas, M. James, Yeeman K. Ramtohul, 2022 .

Crystal and molecular structure of [tris(4,5-diisopropylimidazol-2-yl)phosphine]dichlorozinc(II)-bis[N,N-dimethylformamide]

R. Read, M. James, 1981 .

Serine and threonine beta-lactones: a new class of hepatitis A virus 3C cysteine proteinase inhibitors.

J. Vederas, M. James, Michael N G James, 2002, The Journal of organic chemistry.

The stereoselective synthesis of aziridine analogues of diaminopimelic acid (DAP) and their interaction with dap epimerase.

J. Vederas, M. James, J. Blanchard, 2005, Organic & biomolecular chemistry.

The Molecular and Crystal Structure of an Oxindole Alkaloid (6-Hydroxy-2′-(2-methylpropyl)-3,3′-spirotetrahydropyrrolidino-oxindole)

M. James, G. Williams, 1972 .

M. James, L. Sawyer, M. Robins, 1983 .

The 3C Proteinases of Picornaviruses and Other Positive-Sense, Single-Stranded RNA Viruses

M. James, E. Bergmann, 2000 .

Chemistry of micrococcin P. IX. The crystal and molecular structure of micrococcinic acid bis-4-bromoanilide.

M. James, K. J. Watson, 1966, Journal of the Chemical Society. Perkin transactions 1.

Crystal structure of human beta-hexosaminidase B: understanding the molecular basis of Sandhoff and Tay-Sachs disease.

M. James, B. Mark, S. Knapp, 2003, Journal of molecular biology.

Structural study of the complex between human pepsin and a phosphorus-containing peptidic -transition-state analog.

M. James, M. Fujinaga, N. Tarasova, 2000, Acta crystallographica. Section D, Biological crystallography.

Calcium-binding sites in proteins: a structural perspective.

M. James, C. Mcphalen, N. Strynadka, 1991, Advances in protein chemistry.

ChemInform Abstract: Serine and Threonine β-Lactones: A New Class of Hepatitis A Virus 3C Cysteine Proteinase Inhibitors.

J. Vederas, M. James, Yeeman K. Ramtohul, 2002 .

A refinement of the crystal structure of maleic acid

M. James, G.J.B. Williams, 1974 .

A charge-transfer complex: bis(2,4,6-trimethyl-1-pyridyl)iodonium perchlorate

M. James, G. Brayer, 1982 .

Structural details of a calcium-induced molecular switch: X-ray crystallographic analysis of the calcium-saturated N-terminal domain of troponin C at 1.75 A resolution.

M. James, N. Strynadka, L. Smillie, 1997, Journal of molecular biology.

Lysozyme revisited: crystallographic evidence for distortion of an N-acetylmuramic acid residue bound in site D.

M. James, N. Strynadka, N. J. Strynadka, 1991, Journal of molecular biology.

Refined structure of porcine pepsinogen at 1.8 A resolution.

R J Read, R. Read, M. James, 1991, Journal of molecular biology.

Structure of the complex of Streptomyces griseus proteinase B and polypeptide chymotrypsin inhibitor-1 from Russet Burbank potato tubers at 2.1 A resolution.

M. James, C. Ryan, H. Greenblatt, 1989, Journal of molecular biology.

Refined crystal structure of troponin C from turkey skeletal muscle at 2.0 A resolution.

M. James, O. Herzberg, Osnat Herzberg, 1988, Journal of molecular biology.

Refined structure of alpha-lytic protease at 1.7 A resolution. Analysis of hydrogen bonding and solvent structure.

L. Delbaere, M. James, G. Brayer, 1985, Journal of molecular biology.

Molecular structure of the α-lytic protease from Myxobacter 495 at 2·8 Å resolution☆

L. Delbaere, M. James, G. Brayer, 1979 .

Molecular structure of crystalline Streptomyces griseus protease A at 2.8 A resolution. I. Crystallization, data collection and structural analysis.

L. Delbaere, M. James, G. Brayer, 1978, Journal of molecular biology.

Molecular structure of crystalline Streptomyces griseus protease A at 2.8 A resolution. II. Molecular conformation, comparison with alpha-chymotrypsin and active-site geometry.

L. Delbaere, M. James, G. Brayer, 1978, Journal of molecular biology.

[4]Annulene system. Direct proof for its rectangular geometry

M. James, N. Nakamura, L. Delbaere, 1975 .

Effects of disease-modifying anti-rheumatic drugs (DMARDs) on the activities of rheumatoid arthritis-associated cathepsins K and S

M. James, D. Brömme, Y. Yasuda, 2007, Biological chemistry.

Comparative modeling of the three‐dimensional structure of the calmodulin‐related TCH2 protein from arabidopsis

M. James, K. Johnson, J. Braam, 1997, Proteins.

The molecular and crystal structure of disodium uridine‐3'‐phosphate tetrahydrate

M. James, B. S. Reddy, Viswamitra, 1972 .

The Crystal and Molecular Structure of the Antihistaminic Drug Triprolidine Hydrochloride Monohydrate [trans-1-(p-Tolyl)-1-(2-pyridyl)-3-(1-pyrrolidino)-prop-1-ene]

M. James, G. Williams, 1974 .

Crystal structure of LL-diaminopimelate aminotransferase from Arabidopsis thaliana: a recently discovered enzyme in the biosynthesis of L-lysine by plants and Chlamydia.

J. Vederas, M. James, M. Flegel, 2007, Journal of molecular biology.

Site-directed mutagenesis of histidine 69 and glutamic acid 148 alters the ribonuclease activity of pea ABR17 (PR10.4).

M. James, P. K. Baral, N. Kav, 2011, Plant physiology and biochemistry : PPB.

X-ray crystallographic analyses of complexes between bovine beta-trypsin and Schiff base copper(II) or iron(III) chelates.

M. James, K. Ng, M N James, 2001, Journal of molecular biology.

Biochemical and Structural Assessment of the 1-N-Azasugar GalNAc-isofagomine as a Potent Family 20 β-N-Acetylhexosaminidase Inhibitor*

Stephen G. Withers, Brian L. Mark, S. Withers, 2001, The Journal of Biological Chemistry.

Structures of product and inhibitor complexes of Streptomyces griseus protease A at 1.8 A resolution. A model for serine protease catalysis.

L. Delbaere, M. James, G. Brayer, 1980, Journal of molecular biology.

Effect of pH on the activities of penicillopepsin and Rhizopus pepsin and a proposal for the productive substrate binding mode in penicillopepsin.

R. Hodges, M. James, T. Hofmann, 1984, Biochemistry.

Structural characterization of activation ‘intermediate 2’ on the pathway to human gastricsin

M. James, N. Tarasova, Amir R. Khan, 1997, Nature Structural Biology.

Crystal and molecular structures of human progastricsin at 1.62 A resolution.

M. James, S. Moore, N. Tarasova, 1995, Journal of molecular biology.

Separation of porcine pepsinogen A and progastricsin. Sequencing of the first 73 amino acid residues in progastricsin.

B Foltmann, M. James, M N James, 1992, Biochimica et biophysica acta.

Crystallographic Evidence for Substrate-assisted Catalysis in a Bacterial β-Hexosaminidase*

S. Withers, M. James, D. Vocadlo, 2001, The Journal of Biological Chemistry.

Structure of the complex of Streptomyces griseus protease B and the third domain of the turkey ovomucoid inhibitor at 1.8-A resolution.

R J Read, R. Read, M. James, 1983, Biochemistry.

Aspartate 313 in the Streptomyces plicatusHexosaminidase Plays a Critical Role in Substrate-assisted Catalysis by Orienting the 2-Acetamido Group and Stabilizing the Transition State*

Spencer J. Williams, S. Withers, M. James, 2002, The Journal of Biological Chemistry.

Crystallographic and kinetic investigations of the covalent complex formed by a specific tetrapeptide aldehyde and the serine protease from Streptomyces griseus.

L. Delbaere, M. James, G. Brayer, 1979, Proceedings of the National Academy of Sciences of the United States of America.

Amino acid sequence alignment of bacterial and mammalian pancreatic serine proteases based on topological equivalences.

L. Delbaere, M. James, G. Brayer, 1978, Canadian journal of biochemistry.

Heteroaromatic ester inhibitors of hepatitis A virus 3C proteinase: Evaluation of mode of action

J. Vederas, M. James, L. Eltis, 2008, Bioorganic & Medicinal Chemistry.

Structure-Activity Analysis of Cathepsin K/Chondroitin 4-Sulfate Interactions*

M. James, D. Brömme, F. Lecaille, 2010, The Journal of Biological Chemistry.

Non-nucleoside Analogue Inhibitors Bind to an Allosteric Site on HCV NS5B Polymerase

Meitian Wang, M. James, K. Ng, 2003, The Journal of Biological Chemistry.

The structure of pilocarpine hydrochloride, C11H17N2O2+.Cl−: a muscarinic alkaloid

P. W. Codding, M. James, 1984 .

The molecular geometry of 2',3'-dideoxy-2',3'-didehydroadenosine from an X-ray crystal structure determination

M. James, W. Hutcheon, 1974 .

The crystal and molecular structure of 2,5'-anhydro-2',3'-isopropylidene cyclouridine

L. Delbaere, M. James, 1974 .

The crystal and molecular structures of 2,2'-anhydro-1-β-d-arabino-furanosyl uracil

L. Delbaere, M. James, 1973 .

Molecular structure of troponin C and its implications for the Ca2+ triggering of muscle contraction.

J. Moult, M. James, O. Herzberg, 1987, Methods in enzymology.

A model for the Ca2+-induced conformational transition of troponin C. A trigger for muscle contraction.

J Moult, J. Moult, M. James, 1986, The Journal of biological chemistry.

X-ray crystallography of the binding of the bacterial cell wall trisaccharide NAM-NAG-NAM to lysozyme

D. Phillips, B. Sykes, M. James, 1979, Nature.

Comparative NMR studies on cardiac troponin C and a mutant incapable of binding calcium at site II.

M. James, P. Rosevear, J. Putkey, 1991, Biochemistry.

Crystal and molecular structure of the inhibitor eglin from leeches in complex with subtilisin Carlsberg

M. James, C. Mcphalen, M.N.G. James, 1985, FEBS letters.

Preliminary crystallographic data for the serine protease inhibitor CI-2 from barley seeds.

M. James, C. Mcphalen, K. Hayakawa, 1983, Journal of molecular biology.

Electrostatic reversal of serine proteinase substrate specificity

M. James, A. Caputo, J. Powers, 1999, Proteins.

An Episulfide Cation (Thiiranium Ring) Trapped in the Active Site of HAV 3C Proteinase Inactivated by Peptide-based Ketone Inhibitors

J. Vederas, M. James, L. Eltis, 2006, Journal of Molecular Biology.

Mechanism of acid protease catalysis based on the crystal structure of penicillopepsin

M. James, Michael N. G. James, L. Delbaere, 1977, Nature.

Penicillopepsin from Penicillium janthinellum crystal structure at 2.8 Å and sequence homology with porcine pepsin

M. James, Michael N. G. James, L. Delbaere, 1977, Nature.

Penicillopepsin: 2.8 A structure, active site conformation and mechanistic implications.

L. Delbaere, M. James, T. Hofmann, 1977, Advances in experimental medicine and biology.

Plant protein proteinase inhibitors: structure and mechanism of inhibition.

M. James, K. Bateman, 2011, Current protein & peptide science.

Crystallographic determination of lanthanide ion binding to troponin C

M. James, O. Herzberg, 1986, FEBS letters.

Model for the interaction of amphiphilic helices with troponin C and calmodulin

M. James, N. Strynadka, 1990, Proteins.

CONFORMATIONAL FLEXIBILITY OF TROPONIN C11Supported by the Medical Research Council of Canada, an Alberta Heritage Foundation of Medical Research Fellowship (to O.H.) and an Alberta Heritage Foundation for Medical Research Visiting Scientist Fellowship (to J.M.).

J. Moult, M. James, O. Herzberg, 1987 .

Phosphorylated and dephosphorylated structures of pig heart, GTP-specific succinyl-CoA synthetase.

M. James, W. T. Wolodko, M. Fraser, 2000, Journal of molecular biology.

A detailed structural description of Escherichia coli succinyl-CoA synthetase.

M. James, W. T. Wolodko, M. Fraser, 1999, Journal of molecular biology.

A dimeric form of Escherichia coli succinyl-CoA synthetase produced by site-directed mutagenesis.

M. James, W. T. Wolodko, M. Fraser, 1999, Journal of molecular biology.

A Detailed Structural Description of Escherichia coli

M. James, W. T. Wolodko, M. Fraser, 1999 .

Crystal Structure of the Vitamin B12 Biosynthetic Cobaltochelatase, CbiXS, from Archaeoglobus Fulgidus

M. James, A. Savchenko, J. Walker, 2006, Journal of Structural and Functional Genomics.

Crystal structure of scytalidoglutamic peptidase with its first potent inhibitor provides insights into substrate specificity and catalysis.

M. James, K. Hiraga, K. Oda, 2007, Journal of molecular biology.

The toxicity of antiprion antibodies is mediated by the flexible tail of the prion protein

Tiziana Sonati, Regina R. Reimann, Jeppe Falsig, 2013, Nature.

The peptidases from fungi and viruses

M. James, 2006, Biological chemistry.

Dual Modes of Modification of Hepatitis A Virus 3C Protease by a Serine-derived β-Lactone: Selective Crystallization and Formation of a Functional Catalytic Triad in the Active Site

J. Vederas, M. James, Jiang Yin, 2005, Journal of Molecular Biology.

Conversion of the substrate specificity of mouse proteinase granzyme B

M. James, J. Powers, R. Bleackley, 1994, Nature Structural Biology.

Refined X-ray crystallographic structure of the poliovirus 3C gene product.

M. James, S. Sia, S. Mosimann, 1997, Journal of molecular biology.

Structure determination of Ascaris pepsin inhibitor-3 by MAD phasing

M. James, B. Dunn, K. Ng, 2000 .

Structure of Arterivirus nsp4

M. James, A. Gorbalenya, K. Ng, 2002, The Journal of Biological Chemistry.

Crystal data for tonin, an enzyme involved in the formation of angiotensin II.

M. James, K. Hayakawa, J. A. Kelly, 1978, Journal of molecular biology.

The molecular structure of the complex of Ascaris chymotrypsin/elastase inhibitor with porcine elastase.

M. James, N. Strynadka, Kui Huang, 1994, Structure.

The molecular structure of ornithine acetyltransferase from Mycobacterium tuberculosis bound to ornithine, a competitive inhibitor.

M. James, R. Sankaranarayanan, Chunying Niu, 2010, Journal of molecular biology.

Mechanism of substrate recognition and PLP-induced conformational changes in LL-diaminopimelate aminotransferase from Arabidopsis thaliana.

J. Vederas, M. James, N. Watanabe, 2008, Journal of molecular biology.

Crystal structure of an inhibitor complex of the 3C proteinase from hepatitis A virus (HAV) and implications for the polyprotein processing in HAV.

J. Vederas, M. James, B. Malcolm, 1999, Virology.

Structure and Function of Picornavirus Proteinases

M. James, A. Guarné, T. Skern, 2002 .

Crystallographic structure of human beta-hexosaminidase A: interpretation of Tay-Sachs mutations and loss of GM2 ganglioside hydrolysis.

S. Withers, M. James, M. J. Lemieux, 2006, Journal of molecular biology.

Non-nucleoside inhibitors binding to hepatitis C virus NS5B polymerase reveal a novel mechanism of inhibition.

Meitian Wang, Darius Bilimoria, M. James, 2006, Journal of molecular biology.

Crystal Structures of the RNA-dependent RNA Polymerase Genotype 2a of Hepatitis C Virus Reveal Two Conformations and Suggest Mechanisms of Inhibition by Non-nucleoside Inhibitors*

Meitian Wang, Darius Bilimoria, M. James, 2005, Journal of Biological Chemistry.

Interscaffolding additivity. Association of P1 variants of eglin c and of turkey ovomucoid third domain with serine proteinases.

M. Qasim, M. James, M. Laskowski, 1997, Biochemistry.

Crystal structure of sulfide:quinone oxidoreductase from Acidithiobacillus ferrooxidans: insights into sulfidotrophic respiration and detoxification.

M. James, M. Solomonson, J. Weiner, 2010, Journal of molecular biology.

Dynamics of catalysis revealed from the crystal structures of mutants of diaminopimelate epimerase.

J. Vederas, M. James, J. Blanchard, 2007, Biochemical and biophysical research communications.

Molecular docking programs successfully predict the binding of a beta-lactamase inhibitory protein to TEM-1 beta-lactamase.

R Abagyan, I D Kuntz, M Sternberg, 1996, Nature structural biology.

Protein structure refinement: Streptomyces griseus serine protease A at 1.8 A resolution.

L. Delbaere, M. James, G. Brayer, 1979, Journal of molecular biology.

Studies on the Catalytic Mechanism of a Glutamic Peptidase*

M. James, L. Juliano, M. Juliano, 2010, The Journal of Biological Chemistry.

Structure-activity characterization of sulfide:quinone oxidoreductase variants.

M. James, J. Weiner, Yanfei Zhang, 2012, Journal of structural biology.

Refined 1.7 A X-ray crystallographic structure of P-30 protein, an amphibian ribonuclease with anti-tumor activity.

W. Ardelt, M. James, S. Mosimann, 1994, Journal of molecular biology.

Comparative molecular modeling and crystallization of P‐30 protein: A novel antitumor protein of Rana pipiens oocytes and early embryos

W. Ardelt, M. James, S. Mosimann, 1992, Proteins.

Comparative molecular model building of two serine proteinases from cytotoxic T lymphocytes

I. Weissman, J. Moult, M. James, 1990, Proteins.

The refined crystal structure of the 3C gene product from hepatitis A virus: specific proteinase activity and RNA recognition

M. James, S. Mosimann, B. Malcolm, 1997, Journal of virology.

Molecular mechanisms underlying the interaction of protein phosphatase-1c with ASPP proteins.

M. James, L. Trinkle-Mulcahy, Tamara D. Skene-Arnold, 2013, The Biochemical journal.

Anchimeric assistance in hexosaminidases

M. James, B. Mark, 2002 .

Insights into Mucopolysaccharidosis I from the structure and action of α-L-Iduronidase

Stephen G. Withers, S. Withers, M. James, 2013, Nature chemical biology.

The crystal structure of an octapeptide repeat of the Prion protein in complex with a Fab fragment of the POM2 antibody

A. Aguzzi, M. James, P. K. Baral, 2013, Protein science : a publication of the Protein Society.

Transition of the prion protein from a structured cellular form (PrPC) to the infectious scrapie agent (PrPSc)

A. Aguzzi, M. James, P. K. Baral, 2019, Protein science : a publication of the Protein Society.

Structural characterization of POM6 Fab and mouse prion protein complex identifies key regions for prions conformational conversion

A. Aguzzi, M. James, P. K. Baral, 2018, The FEBS journal.

X-ray structural and molecular dynamical studies of the globular domains of cow, deer, elk and Syrian hamster prion proteins.

A. Aguzzi, M. James, P. K. Baral, 2015, Journal of structural biology.

The structure of the 2A proteinase from a common cold virus: a proteinase responsible for the shut‐off of host‐cell protein synthesis

M. James, E. Kuechler, T. Skern, 1999, The EMBO journal.

Electron density calculations as an extension of protein structure refinement. Streptomyces griseus protease A at 1.5 A resolution.

J Moult, F. Sussman, J. Moult, 1983, Journal of molecular biology.

Crystal structure of the holotoxino from Shigella dysenteriae at 2.5 Å resolution

M. James, M. Fraser, M. Chernaia, 1994, Nature Structural Biology.

Phosphorylation Status of 72 kDa MMP-2 Determines Its Structure and Activity in Response to Peroxynitrite

M. James, P. K. Baral, R. Schulz, 2013, PloS one.

Crystal structure of the yeast cell-cycle control protein, p13suc1, in a strand-exchanged dimer.

M. James, K. Bateman, M. Chernaia, 1996, Structure.

Two trifluoperazine‐binding sites on calmodulin predicted from comparative molecular modeling with troponin‐C

M. James, N. Strynadka, N C Strynadka, 1988, Proteins.

The structure of LL-diaminopimelate aminotransferase from Chlamydia trachomatis: implications for its broad substrate specificity.

J. Vederas, M. James, Chenguang Fan, 2011, Journal of molecular biology.

Molecular dynamics study of the structure and dynamics of a protein molecule in a crystalline ionic environment, Streptomyces griseus protease A.

J Moult, J. Moult, A. Hagler, 1990, Biochemistry.

Crystal and molecular structure of chymotrypsin inhibitor 2 from barley seeds in complex with subtilisin Novo.

M. James, C. Mcphalen, I. Svendsen, 1985, Proceedings of the National Academy of Sciences of the United States of America.

The Crystal Structure of 1-D-myo-Inosityl 2-Acetamido-2-deoxy-α-D-glucopyranoside Deacetylase (MshB) from Mycobacterium tuberculosis Reveals a Zinc Hydrolase with a Lactate Dehydrogenase Fold*

D. Arad, M. James, G. Newton, 2003, Journal of Biological Chemistry.

The molecular structure of Rv1873, a conserved hypothetical protein from Mycobacterium tuberculosis, at 1.38 A resolution.

M. James, C. Garen, E. Bergmann, 2006, Acta crystallographica. Section F, Structural biology and crystallization communications.

Crystallization of a soluble, catalytically active form of Escherichia coli leader peptidase

M. James, M. Paetzel, N. Strynadka, 1995, Proteins.

Structural insights into the activation of P. vivax plasmepsin.

J. Dame, M. James, C. Yowell, 2003, Journal of molecular biology.

The crystal structure of penicillopepsin at 6Åresolution

M. James, S. C. Nyburg, T. Hofmann, 1976 .

Tertiary structural differences between microbial serine proteases and pancreatic serine enzymes

W. E. Thiessen, M. James, L. Delbaere, 1975, Nature.

The crystal structure of the rhomboid peptidase from Haemophilus influenzae provides insight into intramembrane proteolysis

M. James, M. J. Lemieux, K. Bateman, 2007, Proceedings of the National Academy of Sciences.

Crystal structure of N-acetyl-gamma-glutamyl-phosphate reductase from Mycobacterium tuberculosis in complex with NADP(+).

M. James, L. Cherney, Chunying Niu, 2006, Journal of molecular biology.

Structure of the subtilisin Carlsberg-OMTKY3 complex reveals two different ovomucoid conformations.

M. Qasim, M. James, M. Laskowski, 2005, Acta crystallographica. Section D, Biological crystallography.

The molecular structure and catalytic mechanism of a novel carboxyl peptidase from Scytalidium lignicolum.

M. James, M. Fujinaga, K. Oda, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Catalytic pathway of aspartic peptidases

M. James, 2004 .

Unbound Form of Tomato Inhibitor-II Reveals Interdomain Flexibility and Conformational Variability in the Reactive Site Loops*

M. James, K. Ng, G. Pearce, 2003, Journal of Biological Chemistry.

Structural Basis of Inhibition Revealed by a 1:2 Complex of the Two-headed Tomato Inhibitor-II and Subtilisin Carlsberg*

M. James, K. Ng, G. Pearce, 2003, Journal of Biological Chemistry.

Comparison of the solution and X-ray structures of barley serine proteinase inhibitor 2.

A. Gronenborn, G. Clore, M. James, 1987, Protein engineering.

Crystal and molecular structures of the complex of alpha-chymotrypsin with its inhibitor turkey ovomucoid third domain at 1.8 A resolution.

R J Read, R. Read, W. Ardelt, 1987, Journal of molecular biology.

Refined crystal structure of the molecular complex of Streptomyces griseus protease B, a serine protease, with the third domain of the ovomucoid inhibitor from turkey.

R. Read, W. Ardelt, M. James, 1982, Proceedings of the National Academy of Sciences of the United States of America.

Structural basis for the inhibition of porcine pepsin by Ascaris pepsin inhibitor-3

M. James, B. Dunn, K. Ng, 2000, Nature Structural Biology.

Computational analysis of the binding of P1 variants of domain 3 of turkey ovomucoid inhibitor to Streptomyces griseus protease B.

M. James, M. Fujinaga, K. Bateman, 1998, Journal of molecular biology.

1.2A-resolution crystal structures reveal the second tetrahedral intermediates of streptogrisin B (SGPB).

M. James, Michael N G James, Ting-Wai Lee, 2008, Biochimica et biophysica acta.

Structural insights into the non-additivity effects in the sequence-to-reactivity algorithm for serine peptidases and their inhibitors.

M. Qasim, M. James, M. Laskowski, 2007, Journal of molecular biology.

Crystallographic analysis of transition state mimics bound to penicillopepsin: difluorostatine- and difluorostatone-containing peptides.

Michael H. Gelb, M. Gelb, M. James, 1994 .

A detailed description of the structure of Succinyl-COA synthetase from Escherichia coli

M. James, W. T. Wolodko, M. Fraser, 1999 .

Crystal structure of diaminopimelate epimerase from Arabidopsis thaliana, an amino acid racemase critical for L-lysine biosynthesis.

J. Vederas, M. James, S. Marcus, 2009, Journal of molecular biology.

Structural insights into stereochemical inversion by diaminopimelate epimerase: an antibacterial drug target.

J. Vederas, M. James, J. Blanchard, 2006, Proceedings of the National Academy of Sciences of the United States of America.

Stereochemical analysis of peptide bond hydrolysis catalyzed by the aspartic proteinase penicillopepsin.

M. James, A. Sielecki, A R Sielecki, 1985, Biochemistry.

Carboxyl–carboxylate interactions in proteins

Lindsay Sawyer, M. James, L. Sawyer, 1982, Nature.

Structural and Functional Characterization of Streptomyces plicatus β-N-Acetylhexosaminidase by Comparative Molecular Modeling and Site-directed Mutagenesis*

M. James, P. Robbins, B. Mark, 1998, The Journal of Biological Chemistry.

Crystallization and preliminary X‐ray diffraction studies of two mutants of lactate dehydrogenase from Bacillus stearothermophilus

R. Kodandapani, M. James, J. B. Jones, 1992, Proteins.

Crystal structures of protein phosphatase-1 bound to motuporin and dihydromicrocystin-LA: elucidation of the mechanism of enzyme inhibition by cyanobacterial toxins.

M. James, David E. Williams, R. Andersen, 2006, Journal of molecular biology.

Common structural features of the luxF protein and the subunits of bacterial luciferase: Evidence for a (βα)8 fold in luciferase

M. James, S. Moore, 1994, Protein science : a publication of the Protein Society.

Probing the nucleotide-binding site of Escherichia coli succinyl-CoA synthetase.

M. James, W. T. Wolodko, M. Fraser, 1999, Biochemistry.

Crystallization of succinyl-CoA synthetase from Escherichia coli.

M. James, W. T. Wolodko, W. A. Bridger, 1984, The Journal of biological chemistry.

Structural refinement of the non-fluorescent flavoprotein from Photobacterium leiognathi at 1.60 A resolution.

M. James, S. Moore, M N James, 1995, Journal of molecular biology.

Crystal structure of a flavoprotein related to the subunits of bacterial luciferase.

M. James, D. O'Kane, J. Lee, 1993, EMBO Journal.

Active Site of α-Lytic Protease

M. James, G. Brayer, C. Bauer, 1981 .

The 2.8 A resolution structure of Streptomyces griseus protease B and its homology with alpha-chymotrypsin and Streptomyces griseus protease A.

L. Delbaere, M. James, G. Brayer, 1979, Canadian Journal of Biochemistry.

The molecular structure of epoxide hydrolase B from Mycobacterium tuberculosis and its complex with a urea-based inhibitor.

M. James, B. Hammock, C. Morisseau, 2008, Journal of molecular biology.

Calcium binding to skeletal muscle troponin C and the regulation of muscle contraction.

J. Moult, M. James, O. Herzberg, 2007, Ciba Foundation symposium.

Structural insights for the substrate recognition mechanism of LL-diaminopimelate aminotransferase.

M. James, N. Watanabe, 2011, Biochimica et biophysica acta.

The crystal structure of Rv0793, a hypothetical monooxygenase from M.␣tuberculosis

M. James, M. J. Lemieux, C. Garen, 2006, Journal of Structural and Functional Genomics.

Towards an understanding of the effects of calcium on protein structure and function

M. James, N. Strynadka, 1991, Current Biology.

X-ray crystal structure of Mycobacterium tuberculosis haloalkane dehalogenase Rv2579.

M. James, C. Garen, M. Cherney, 2008, Biochimica et biophysica acta.

Cloning, expression, purification, crystallization and preliminary X-ray studies of epoxide hydrolases A and B from Mycobacterium tuberculosis.

M. James, C. Garen, M. Cherney, 2006, Acta crystallographica. Section F, Structural biology and crystallization communications.

Crystal structure of the novel aspartic proteinase zymogen proplasmepsin II from Plasmodium falciparum

Robert G. Ridley, M. James, H. Loetscher, 1999, Nature Structural Biology.

Structure of Shiga Toxin Type 2 (Stx2) from Escherichia coli O157:H7*

M. James, M. Fujinaga, M. Fraser, 2004, Journal of Biological Chemistry.

Conformational flexibility in the active sites of aspartyl proteinases revealed by a pepstatin fragment binding to penicillopepsin.

M. James, F. Salituro, D. Rich, 1982, Proceedings of the National Academy of Sciences of the United States of America.

The POM Monoclonals: A Comprehensive Set of Antibodies to Non-Overlapping Prion Protein Epitopes

S. Hornemann, A. Aguzzi, M. James, 2008, PloS one.

Expression, purification and preliminary crystallographic analysis of Rv2247, the β subunit of acyl-CoA carboxylase (ACCD6) from Mycobacterium tuberculosis.

M. James, Jiang Yin, Chunying Niu, 2011, Acta crystallographica. Section F, Structural biology and crystallization communications.

The Crystal Structure of Shiga Toxin Type 2 with Bound Disaccharide Guides the Design of a Heterobifunctional Toxin Inhibitor*

M. James, G. Armstrong, Jiang Yin, 2013, The Journal of Biological Chemistry.

Molecular mechanisms underlying the interaction of protein phosphatase-1 c with ASPP proteins

M. James, L. Trinkle-Mulcahy, Tamara D. Skene-Arnold, 2012 .

Binding of adenine to Stx2, the protein toxin from Escherichia coli O157:H7.

M. James, P. Marcato, G. Armstrong, 2006, Acta crystallographica. Section F, Structural biology and crystallization communications.

A Mechanistic View of Enzyme Inhibition and Peptide Hydrolysis in the Active Site of the SARS-CoV 3C-like Peptidase

J. Vederas, M. James, L. Eltis, 2007, Journal of Molecular Biology.

Crystal structure of gamma-chymotrypsin in complex with 7-hydroxycoumarin.

M. James, K. Ng, Atta-ur-rahman, 2001, Journal of molecular biology.

Critical evaluation of comparative model building of Streptomyces griseus trypsin.

R J Read, R. Read, M. James, 1984, Biochemistry.

Accurate dimensions of the maleate mono-anion in a symmetric environment not dictated by crystallographic symmetry: imidazolium maleate

M. James, M. Matsushima, 1976 .

Crystal structure and nucleotide sequence of an anionic trypsin from chum salmon (Oncorhynchus keta) in comparison with Atlantic salmon (Salmo salar) and bovine trypsin.

M. James, K. Ng, S. Kuninaga, 2002, Journal of molecular biology.

Structure of arterivirus nsp4-The smallest chymotrypsin- like protease with an / -C-terminal extension and alternate conformations of the oxyanion hole

M. James, A. Gorbalenya, K. Ng, 2008 .

Crystal Structure and Mutagenesis of a Protein Phosphatase-1:Calcineurin Hybrid Elucidate the Role of the β12-β13 Loop in Inhibitor Binding*

M. James, C. Holmes, J. Maynes, 2004, Journal of Biological Chemistry.

Structure of (+)‐(5R,6R)‐5‐Chloro‐6‐methoxy‐5,6‐dihydro‐1‐(2′,3′‐ didehydro‐2′,3′‐dideoxy‐β‐D‐glycero‐2‐enopentofuranosyl)thymine

M. James, H. Blanchard, L. Wiebe, 1993 .

X-ray diffraction studies on penicillopepsin and its complexes: the hydrolytic mechanism

M. James, A. Sielecki, T. Hofmann, 1985 .

Structure of (+)-(5R,6R)-5-chloro-6-methoxy-5,6-dihydro-1-(2',3'-didehydro-2',3'-dideoxy-β-d-glycero-2-enopentofuranosyl)thymine

M. James, H. Blanchard, Rakesh Kumar, 1993 .

Expression, purification and preliminary crystallographic analysis of O-acetylhomoserine sulfhydrylase from Mycobacterium tuberculosis.

M. James, L. Hung, J. Habel, 2011, Acta crystallographica. Section F, Structural biology and crystallization communications.

Crystal structure of β-hexosaminidase B in complex with pyrimethamine, a potential pharmacological chaperone.

M. James, K. Bateman, D. Mahuran, 2011, Journal of medicinal chemistry.

Two trifluoperazine‐binding sites on calmodulin predicted from comparative molecular modeling with troponin‐C

M. James, N. Strynadka, 1988, Proteins.

Structural Studies of Histamine H1 Effector Molecules: The Crystal Structure of the Antihistamine Drug (+)-Chlorpheniramine Maleate; [(+)-S-1-(p-Chlorophenyl)-1-(2-pyridyl)-3-N,N-dimethylpropylamine maleate]

M. James, G. Williams, 1974 .

The Molecular Conformation of 1e,2a,6e-Trimethyl-4e-phenyl-4a-acetoxypiperidine Hydrobomide in the Crystalline State

M. James, K. Hayakawa, 1973 .

Crystal structure of N-Methyl-N-phenylretinal iminium perchlorate: A structural model for the bacteriorhodopsin chromophore

M. James, B. Santarsiero, R. F. Childs, 1990 .

The structures of picornaviral proteinases.

M. James, W. Sommergruber, A. Guarné, 1999, Virus research.

A detailed structural description of escherichia coli succinly-CoA synthetase

Fraser, M. James, W. T. Wolodko, 1999, Journal of molecular biology.

Design, synthesis, and evaluation of inhibitors for severe acute respiratory syndrome 3C-like protease based on phthalhydrazide ketones or heteroaromatic esters.

J. Vederas, M. James, L. Eltis, 2007, Journal of medicinal chemistry.

Crystal structure of the intermediate complex of the arginine repressor from Mycobacterium tuberculosis bound with its DNA operator reveals detailed mechanism of arginine repression.

M. James, L. Cherney, C. Garen, 2010, Journal of molecular biology.

The 4.5 Å Resolution Structure of a Bacterial Serine Protease from Streptomyces Griseus

L. Delbaere, P. W. Codding, M. James, 1974 .

RELATIONSHIP BETWEEN THE STRUCTURES AND ACTIVITIES OF SOME MICROBIAL SERINE PROTEASES. II. COMPARISON OF THE TERTIARY STRUCTURES OF MICROBIAL AND PANCREATIC SERINE PROTEASES

M. James, 1976 .

The crystal structure of the arsenite complex of dithiothreitol

M. James, W. Cruse, 1972 .

Crystal structure of the arginine repressor protein in complex with the DNA operator from Mycobacterium tuberculosis.

M. James, George J. Lu, L. Cherney, 2008, Journal of molecular biology.

Structure of the C-terminal domain of the arginine repressor protein from Mycobacterium tuberculosis.

M. James, George J. Lu, L. Cherney, 2008, Acta crystallographica. Section D, Biological crystallography.

Expression, purification and preliminary X-ray analysis of the C-terminal domain of an arginine repressor protein from Mycobacterium tuberculosis.

M. James, George J. Lu, L. Cherney, 2007, Acta Crystallographica. Section F : Structural Biology and Crystallization Communications.

Structural studies on the folded domain of the human prion protein bound to the Fab fragment of the antibody POM1.

Pravas Kumar Baral, Mridula Swayampakula, Barbara Wieland, 2012, Acta crystallographica. Section D, Biological crystallography.

Crystallization and preliminary X-ray diffraction analysis of prion protein bound to the Fab fragment of the POM1 antibody.

A. Aguzzi, M. James, P. K. Baral, 2011, Acta crystallographica. Section F, Structural biology and crystallization communications.

Expression, purification and preliminary crystallographic analysis of N-acetylglucosamine-1-phosphate uridylyltransferase from Mycobacterium tuberculosis.

M. James, Jiang Yin, L. Cherney, 2008, Acta crystallographica. Section F, Structural biology and crystallization communications.

Macrocyclic Inhibitors of Penicillopepsin. 2. X-ray Crystallographic Analyses of Penicillopepsin Complexed with a P3−P1 Macrocyclic Peptidyl Inhibitor and with Its Two Acyclic Analogues

M. James, M. Fraser, P. Bartlett, 1998 .

The crystal structure of 2,2'-anhydro-2-hydroxy-1-(β-d-arabino-pentofuranosyl)4-pyridone

M. James, W. Hutcheon, 1977 .

The crystal structure of 3‐deazacytidine

M. James, W. Hutcheon, 1977 .

The molecular and crystal structure of N-(-D-ribofuranosyl)imidazole

M. James, M. Matsushima, 1973 .

Crystallographic analysis of transition-state mimics bound to penicillopepsin: phosphorus-containing peptide analogues.

M. James, N. Strynadka, J. Hanson, 1993, Biochemistry.

Crystallographic data for troponin C from turkey skeletal muscle.

M. James, O. Herzberg, K. Hayakawa, 1984, Journal of molecular biology.

Crystal Structures Reveal an Induced-fit Binding of a Substrate-like Aza-peptide Epoxide to SARS Coronavirus Main Peptidase

M. James, L. Eltis, Jie Liu, 2006, Journal of Molecular Biology.

Analysis and prediction of solvent structures in protein crystals

J. Moult, M. James, A. Sielecki, 1984 .

Crystallographic analysis of transition state mimics bound to penicillopepsin: difluorostatine- and difluorostatone-containing peptides.

M. Gelb, M. James, K. Hayakawa, 1994 .

Cysteine proteases: evolution, function, and inhibitor design.

M. James, J. McKerrow, 1996 .

Crystal structure of Mycobacterium tuberculosis Rv0760c at 1.50 A resolution, a structural homolog of Delta(5)-3-ketosteroid isomerase.

M. James, C. Garen, M. Cherney, 2008, Biochimica et biophysica acta.